Canonical Allele Identifier: CA2673260093

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385145-T-TGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385146_11385148dup , CM000667.2:g.11385146_11385148dup	GRCh38
NC_000005.9:g.11385258_11385260dup , CM000667.1:g.11385258_11385260dup	GRCh37
NC_000005.8:g.11438258_11438260dup	NCBI36
NG_023544.1:g.523851_523853dup
NG_023544.2:g.523851_523853dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20258_167-20256dup	ENSP00000516315.1:n.167-20258_167-20256dup
ENST00000304623.13:c.694_696dup MANE Select	ENSP00000307134.8:p.Pro232_Ser233insPro
ENST00000304623.12:c.694_696dup	ENSP00000307134.8:p.Pro232_Ser233insPro
ENST00000502551.5:c.398-20258_398-20256dup	ENSP00000422389.1:n.398-20258_398-20256dup
ENST00000503622.5:c.167-20258_167-20256dup	ENSP00000426887.1:n.167-20258_167-20256dup
ENST00000504354.5:n.217-20258_217-20256dup
ENST00000504499.5:c.612+11883_612+11885dup	ENSP00000421000.1:n.612+11883_612+11885dup
ENST00000511278.5:n.542-20258_542-20256dup
ENST00000511377.5:c.421_423dup	ENSP00000426510.1:p.Pro141_Ser142insPro
ENST00000513588.5:c.440-20258_440-20256dup	ENSP00000421093.1:n.440-20258_440-20256dup
ENST00000513598.5:c.421_423dup	ENSP00000426625.1:p.Pro141_Ser142insPro
ENST00000514132.1:n.343_345dup
NM_001288715.1:c.421_423dup	NP_001275644.1:p.Pro141_Ser142insPro
NM_001288716.1:c.167-20258_167-20256dup	NP_001275645.1:n.167-20258_167-20256dup
NM_001288717.1:c.-123+11883_-123+11885dup	NP_001275646.1:n.-123+11883_-123+11885dup
NM_001332.3:c.694_696dup	NP_001323.1:p.Pro232_Ser233insPro
NR_109988.1:n.630-20258_630-20256dup
XM_005248251.2:c.694_696dup	XP_005248308.1:p.Pro232_Ser233insPro
XM_005248252.1:c.652_654dup	XP_005248309.1:p.Pro218_Ser219insPro
XM_005248253.1:c.421_423dup	XP_005248310.1:p.Pro141_Ser142insPro
XM_011513967.1:c.421_423dup	XP_011512269.1:p.Pro141_Ser142insPro
NM_001364128.1:c.167-20258_167-20256dup	NP_001351057.1:n.167-20258_167-20256dup
XM_005248251.3:c.694_696dup	XP_005248308.1:p.Pro232_Ser233insPro
XM_005248252.2:c.652_654dup	XP_005248309.1:p.Pro218_Ser219insPro
XM_011513967.2:c.421_423dup	XP_011512269.1:p.Pro141_Ser142insPro
XM_017009072.1:c.440-20258_440-20256dup	XP_016864561.1:n.440-20258_440-20256dup
XM_017009073.1:c.398-20258_398-20256dup	XP_016864562.1:n.398-20258_398-20256dup
XM_017009074.1:c.440-20258_440-20256dup	XP_016864563.1:n.440-20258_440-20256dup
XM_017009075.2:c.167-20258_167-20256dup	XP_016864564.1:n.167-20258_167-20256dup
NM_001332.4:c.694_696dup MANE Select	NP_001323.1:p.Pro232_Ser233insPro
NM_001288717.2:c.-123+11883_-123+11885dup	NP_001275646.1:n.-123+11883_-123+11885dup
NR_109988.2:n.1033-20258_1033-20256dup
NM_001364128.2:c.167-20258_167-20256dup	NP_001351057.1:n.167-20258_167-20256dup